Unravelling in-situ formation of highly active mixed metal oxide CuInO2 nanoparticles during CO2 electroreduction

被引:30
|
作者
Imani, Roghayeh [1 ,2 ]
Qiu, Zhen [3 ]
Younesi, Reza [2 ]
Pazoki, Meysam [2 ,3 ]
Fernandes, Daniel L. A. [1 ]
Mitev, Pavlin D. [2 ]
Edvinsson, Tomas [3 ]
Tian, Haining [1 ]
机构
[1] Uppsala Univ, Dept Chem, Phys Chem, Angstrom Lab, Box 523, S-75120 Uppsala, Sweden
[2] Uppsala Univ, Dept Chem, Struct Chem, Angstrom Lab, Box 538, S-75121 Uppsala, Sweden
[3] Uppsala Univ, Dept Engn Sci, Solid State Phys Div, Angstrom Lab, Box 534, S-75121 Uppsala, Sweden
关键词
Cuprous oxide; Copper indium oxide; CO2; electroreduction; Operando Raman spectroelectrochemistry; Density functional theory; DIFFUSION-DRIVEN; COPPER; RAMAN; ELECTRODES; REDUCTION; CU2O; FUEL; INTERFACES; INDIUM;
D O I
10.1016/j.nanoen.2018.04.013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Technologies and catalysts for converting carbon dioxide (CO2) to immobile products are of high interest to minimize greenhouse effects. Copper(I) is a promising catalytic active state of copper but hampered by the inherent instability in comparison to copper(II) or copper(0). Here, we report a stabilization of the catalytic active state of copper(I) by the formation of a mixed metal oxide CuInO2 nanoparticle during the CO2 electroreduction. Our result shows the incorporation of nanoporous Sn:In2O3 interlayer to Cu2O pre-catalyst system lead to the formation of CuInO2 nanoparticles with remarkably higher activity for CO2 electroreduction at lower overpotential in comparison to the conventional Cu nanoparticles derived from sole Cu2O. Operando Raman spectroelectrochemistry is employed to in-situ monitor the process of nanoparticles formation during the electrocatalytic process. The experimental data are collaborated with DFT calculations to provide insight into the electro-formation of the type of Cu-based mixed metal oxide catalyst during the CO2 electroreduction, where a formation mechanism via copper ion diffusion across the substrate is suggested.
引用
收藏
页码:40 / 50
页数:11
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